A Clinical Trial to evaluate AL002 in Participants with early Alzheimer's Disease

Phase 1

• Conditions: Early Alzheimer's Disease; MedDRA version: 20.0Level: SOCClassification code 10029205Term: Nervous system disordersSystem Organ Class: 10029205 - Nervous system disorders; Therapeutic area: Diseases [C] - Nervous System Diseases [C10]

• Registration Number: EUCTR2022-002987-57-DE
• Lead Sponsor: Alector, Inc.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-01-12
• Last Update Posted: 26 February 2024

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 190

Inclusion Criteria

1. The participant has completed the Planned Treatment Period in the AL002-2 study. Completion of the Planned Treatment Period is defined as any participant who did not prematurely and permanently discontinue IMP in the AL002-2 study.
2. The participant is willing and able to give informed consent. Where local regulations permit inclusion of participants deemed not able to provide informed consent, a legally authorized representative must provide informed consent on his or her behalf, and the participant must provide assent, in accordance with the local regulations, guidelines, and institutional review board or independent ethics committee.
3. The participant has availability of a person (study partner”) who, in the Investigator’s opinion, has frequent and sufficient contact with the participant (eg, at least 10 hours per week of in person contact), is able to provide accurate information regarding the participant’s cognitive and functional abilities, agrees to provide information at clinic visits (which require partner input for scale completion), and signs the necessary consent form.
a. The study partner must have sufficient cognitive capacity, in the Investigator’s opinion, to accurately report upon the participant’s behavior, cognitive, and functional abilities. The study partner should be in sufficiently good general health, in the Investigator’s opinion, to have a high likelihood of maintaining the same level of interaction with the participant and participation in study procedures throughout the study duration.
b. Every effort should be made to have the same study partner participate throughout the duration of the study, and to have the same study partner as in the parent study.
4. The participant and study partner are fluent in the language of the tests used at the study site as assessed by site personnel.
5. The participant is willing and able to complete all aspects of the study (including MRI, optional LP, genotyping, and optional PET imaging, as applicable). The participant should be capable of completing assessments either alone or with the help of the study partner.
6. The participant has adequate visual and auditory acuity, in the Investigator’s opinion, sufficient to perform the neuropsychological testing (corrective lenses and hearing aids are permitted).
7. Participant agrees not to donate blood or blood products for transfusion for the duration of the study and for 1 year after the final dose of study drug.
Inclusion criteria for participants in the optional tau PET imaging assessment with [18F]MK-6240 only:
8. Participant has not had excessive radiation exposure prior to enrollment in the trial, as defined by local standards.
9. [18F]MK-6240 is available to the PET imaging center based on manufacturing distribution network and local regulations.
Inclusion criteria for participants in the optional longitudinal amyloid PET imaging assessment only:
10. Participant has not had excessive radiation exposure prior to enrollment in the trial, as defined by local standards.
11. An approved amyloid radiotracer is available to the PET imaging center based on manufacturing distribution network and local regulations.
Inclusion criteria for participants in the optional at-home and/or in-clinic WLSA only:
12. For at-home participation:
a. Participant has an available and willing study partner to administer the WLSA.
b. Participant has WiFi access in their residence or WiFi access in a private area where the testing can take pla

Exclusion Criteria

Participants deemed not able to provide consent or assent by the Investigator or by local regulations.
2. Participants who were prematurely and permanently discontinued from treatment in the parent
study for safety reasons. 3. The participant has MRI evidence of:
a. >2 lacunar infarcts.
b. Any territorial infarct >1 cm3.
c. White matter hyperintense lesions on the FLAIR sequence that correspond to an overall Fazekas score of 3.
d. Participants who have an increase in their number of microbleeds, since the previous screening/ baseline MRI in the AL002-2 study and >5, should be discussed with the Medical Monitor.
e. Participants who have developed ARIA-E and ARIA-H in the parent study and who were permitted to continue dosing according to the ARIA management guidelines, will not be excluded from participation in the AL002-LTE, on the basis of microbleeds or hemosiderosis.
4. Participation in the AL002-LTE is deemed inappropriate for any reason per Investigator discretion.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified